C0543541[trait identifier] AND "Neuberg Centre For Genomic Medicine, N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 345394	NM_020208.4(SLC6A20):c.1742G>A (p.Arg581His)	SLC6A20 (R581H +1 more)	Single nucleotide variant (missense variant)	Hyperglycinuria +1 more	GUncertain significance
Select item 2585140	NM_001003841.3(SLC6A19):c.774+2T>G	SLC6A19	Single nucleotide variant (splice donor variant)	Hyperglycinuria	GLikely pathogenic
Select item 2584784	NM_001003841.3(SLC6A19):c.1228A>G (p.Met410Val)	SLC6A19 (M410V)	Single nucleotide variant (missense variant)	Hyperglycinuria	GUncertain significance

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